TY  - GEN
AU  - Kantaputra,Piranit N
AU  - Limwongse,Chanin
AU  - Tochareontanaphol,Chintana
AU  - Mutirangura,Apiwat
AU  - Mevatee,Umnat
AU  - Praphanphoj,Verayuth
TI  - Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: association with an 18p11.3 deletion
SN  - 1552-4825
PY  - 2007///0220
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adult
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 18
KW  - Holoprosencephaly
KW  - diagnosis
KW  - Homeodomain Proteins
KW  - Humans
KW  - Hypotrichosis
KW  - Intellectual Disability
KW  - Karyotyping
KW  - Male
KW  - Microcephaly
KW  - Phenotype
KW  - Repressor Proteins
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.31386
ER  -